KRT8

GENERAL INFORMATION

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Gene name

KRT8

Gene description

Keratin 8

Protein class

Cancer-related genes
Disease related genes
Plasma proteins
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

9
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (small intestine)
GTEx:Tissue enhanced (colon, small intestine)

Protein evidence

Evidence at protein level

Protein localization

Cytoplasmic and membranous expression in glandular epithelium.

ANTIBODY RELIABILITY

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Data reliability
description

Antibody staining mainly consistent with RNA expression data. Caution, targets protein from more than one gene.

Data reliability

Supportive based on 3 antibodies.
HPA049866 , CAB000131 , CAB001696
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis

Prostate



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enhanced (small intestine)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (colon, small intestine)

Organ

Expression



GENE INFORMATION

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Gene name

KRT8 (HGNC Symbol)

Synonyms

CARD2, CK8, CYK8, K2C8, K8, KO

Description

Keratin 8 (HGNC Symbol)

Entrez gene summary

This gene is a member of the type II keratin family clustered on the long arm of chromosome 12. Type I and type II keratins heteropolymerize to form intermediate-sized filaments in the cytoplasm of epithelial cells. The product of this gene typically dimerizes with keratin 18 to form an intermediate filament in simple single-layered epithelial cells. This protein plays a role in maintaining cellular structural integrity and also functions in signal transduction and cellular differentiation. Mutations in this gene cause cryptogenic cirrhosis. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012]

Chromosome

12

Cytoband

q13.13

Chromosome location (bp)

52897187 - 52949954

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000170421 (version 78.38)

Entrez gene

3856

UniProt

P05787 (UniProt - Evidence at protein level)

neXtProt

NX_P05787

Antibodypedia

KRT8 antibodies


PROTEIN BROWSER

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ENST00000293308
 
ENST00000546542
 
ENST00000546826
 
ENST00000546897
 
ENST00000546900
 
ENST00000547413
 
ENST00000548998
 
ENST00000552150
 
ENST00000552551
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

KRT8-001 ENSP00000447566
ENST00000552551
P05787
Show all »
Show » Show » 483 53.7 No 0
KRT8-002 ENSP00000293308
ENST00000293308
P05787
Show all »
Show » Show » 483 53.7 No 0
KRT8-003 ENSP00000447402
ENST00000546897
P05787
Show all »
Show » Show » 483 53.7 No 0
KRT8-004 ENSP00000449404
ENST00000552150
P05787
Show all »
Show » Show » 511 56.6 No 0
KRT8-013 ENSP00000447881
ENST00000546826
F8VUG2
Show all »
Show » Show » 273 30.9 No 0
KRT8-014 ENSP00000447040
ENST00000548998
F8W1U3
Show all »
Show » Show » 289 32.5 No 0
KRT8-015 ENSP00000450228
ENST00000546542
F8VQY3
Show all »
Show » Show » 180 19.1 No 0
KRT8-016 ENSP00000448681
ENST00000547413
F8VRG4
Show all »
Show » Show » 177 19.6 No 0
KRT8-017 ENSP00000450340
ENST00000546900
F8VP67
Show all »
Show » Show » 113 13.6 No 0